research on retinal degeneration

我们分析了视网膜变性的致病基因。我们在Bietti晶体视网膜病变中发现了几个外周蛋白rds基因或CYP4 V2基因的突变。在x连锁色素性视网膜炎基因患者中，我们分析了RPGR基因和RP2基因的ORF15区域。我们对RS-1基因突变的先天性视网膜裂患者进行玻璃体手术并报告结果。我们还建立了缺血性视神经病变的实验模型，成功地记录了STR。STR的记录显示了视网膜内功能。

We analysed causative genes of retinal degenertions. We have found several mutations in peripherin-RDSgene or CYP4 V2 gene of Bietti crystalline retinopathy. In x-linked retinitis pigmentosa gene patients, we analysed ORF15 region of RPGR gene and RP2 gene. In congenital retinoschisis patients with RS-1 gene mutation, we performed vitreous surgeries and reported the results.We also established experimental model of ischemic optic neuropathy and successfully recorded STR. Recording of STR revealed innner retinal function.